Chimeric Antigen Receptor T-Cell Postinfusion Fever: Infection Profile, Clinical Parameters, and Biomarkers Trends to Assist Antibiotic Stewardship

Author:

Peyrony Olivier12ORCID,Garcia-Pouton Nicole3,Chumbita Mariana3,Teijon-Lumbreras Christian3,Aiello Tommaso Francesco3,Monzó-Gallo Patricia3,Gallardo-Pizarro Antonio3,Ortiz-Maldonado Valentín4ORCID,Martinez-Cibrian Núria4,Delgado Julio4ORCID,Fernandez de Larrea Carlos4,Mensa Josep3,Puerta-Alcalde Pedro3ORCID,Soriano Alex35ORCID,Garcia-Vidal Carolina3

Affiliation:

1. Department of Infectious Diseases, Hospital Clinic of Barcelona , Barcelona , Spain

2. Emergency Department, Hôpital Saint-Louis, Assistance Publique–Hôpitaux de Paris , Paris , France

3. Department of Infectious Diseases, Hospital Clinic of Barcelona, Instituto de Investigaciones Biomédicas August Pi i Sunyer, University of Barcelona , Barcelona , Spain

4. Department of Hematology, Hospital Clinic of Barcelona, Instituto de Investigaciones Biomédicas August Pi i Sunyer, University of Barcelona , Barcelona , Spain

5. CIBERINFECT, Centro de Investigación Biomédica en Red, Instituto de Salud Carlos III , Madrid , Spain

Abstract

Abstract Background This study aimed to describe documented infections associated with postinfusion fever after CAR T-cell therapy and to evaluate daily changes in vital signs, laboratory results, and the National Early Warning Score (NEWS) in patients with and without confirmed bacterial infections following fever onset, with the objective of assisting in antibiotic stewardship. Methods This was a retrospective, observational study including all consecutive adult patients who received CAR T-cell therapy. Documented infection in the first fever episode after infusion, and clinical and analytic trend comparison of patients with bacterial documented infections and those without documented infections, are described. Results Among 152 patients treated with CAR T-cell therapy, 87 (57.2%) had fever within 30 days of infusion, with a median time from infusion to fever of 3 (interquartile range, 2–5) days. Of these 87 patients, 82 (94.3%) received broad-spectrum antibiotics. Infection was documented in 9 (10.3%) patients and only 4 (4.6%) had bacterial infections. Clinical signs and biomarkers were similar in patients with bacterial documented infection and in those without documented infection at fever onset. Fever, tachycardia, and high C-reactive protein levels remained high during the first 3 days after CAR T-cell infusion, even when no infection was documented. Conclusions Fever is a common symptom following CAR T-cell infusion and is largely treated with broad-spectrum antibiotics. However, confirmed bacterial documented infections after the first fever post–CAR T-cell infusion are very unusual. Because clinical parameters and biomarkers are not useful for identifying infectious fever, other methods should be assessed to ensure the proper use of antibiotics.

Funder

European Regional Development Fund

Instituto de Salud Carlos III

European Union

Spanish Ministry of Health

Red de Terapia Celular TerCel

'la Caixa' Foundation

Asociación Española Contra el Cancer

Publisher

Oxford University Press (OUP)

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